Agee J F, Garver F A, Faguet G B
Blood. 1986 Jul;68(1):62-8.
Rabbit xenoantisera and mouse monoclonal antibodies prepared against human chronic lymphocytic leukemia (CLL) B cells were found to react against a single polypeptide chain with a mol wt of 69 kd found on leukemic cells of all CLL (N = 40) and B type hairy cell leukemia (HCL) patients (N = 9) examined. This common CLL-associated antigen (cCLLa) was not detectable on circulating T or B lymphocytes, thymocytes, lymph node and splenic lymphocytes, or bone marrow leukocytes from normal persons. In addition, the cCLLa was not detectable on cultured T or B lymphoblastoid cell lines or on malignant cells from other forms of lymphocytic or myelocytic leukemia. Non-Hodgkin's lymphoma cells also failed to express the antigen. Autologous cultured lymphoblastoid cell lines were established from residual normal B cells from a CLL patient whose cells were used to generate one of the antisera. Absorption of the antibody with these cultured polyclonal B cells did not affect the anti-CLL activity, which suggests that the cCLLa is not HLA related. Unlike the T cell differentiation complex gp65-71, the cCLLa was not expressed on fetal or cord blood lymphocytes or on mitogen-stimulated normal lymphocytes and was distinct from the antigen recognized by the LEU-1 antibody in spite of their similar mol wt. The cCLLa was also determined to be unrelated to the human T cell leukemia lymphoma virus (HTLV-1). One of the monoclonal antibodies generated against the cCLLa was a complement binding IgG which exhibited highly selective cytotoxic activity against 100% of cells bearing the cCLLa. Such an antibody might prove clinically useful in early diagnosis and treatment of CLL and HCL.
针对人类慢性淋巴细胞白血病(CLL)B细胞制备的兔异种抗血清和小鼠单克隆抗体,被发现可与一条分子量为69kd的单多肽链发生反应,该多肽链存在于所有接受检测的CLL患者(N = 40)和B型毛细胞白血病(HCL)患者(N = 9)的白血病细胞上。这种常见的CLL相关抗原(cCLLa)在正常人的循环T或B淋巴细胞、胸腺细胞、淋巴结和脾淋巴细胞或骨髓白细胞上无法检测到。此外,在培养的T或B淋巴母细胞系或其他形式的淋巴细胞性或髓细胞性白血病的恶性细胞上也检测不到cCLLa。非霍奇金淋巴瘤细胞也不表达该抗原。从一名CLL患者残留的正常B细胞中建立了自体培养的淋巴母细胞系,该患者的细胞被用于制备其中一种抗血清。用这些培养的多克隆B细胞吸收抗体并不影响其抗CLL活性,这表明cCLLa与HLA无关。与T细胞分化复合物gp65 - 71不同,cCLLa在胎儿或脐血淋巴细胞或有丝分裂原刺激的正常淋巴细胞上不表达,尽管它们的分子量相似,但与LEU - 1抗体识别的抗原不同。cCLLa也被确定与人类T细胞白血病淋巴瘤病毒(HTLV - 1)无关。针对cCLLa产生的一种单克隆抗体是一种补体结合IgG,它对100%携带cCLLa的细胞表现出高度选择性的细胞毒性活性。这样一种抗体可能在CLL和HCL的早期诊断和治疗中具有临床应用价值。